Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,479 positions on this site are linked to Height, out of 2,509,486 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

near GTF2H3 · rs150792771

See detailed info → Standard

Height (baseline)

CEP112 · rs148762808

See detailed info → Standard

Height (baseline)

CNNM2 · rs148650436

See detailed info → Standard

Height (baseline)

CYBRD1 · rs147506462

See detailed info → Standard

Height

PDZRN4 · rs147299042

See detailed info → Standard

Height (baseline)

near LRP4 · rs146409168

See detailed info → Standard

Height

TMEM71 · rs145103289

See detailed info → Standard

Height (baseline)

near RN7SL316P · rs144845777

See detailed info → Standard

Height (baseline)

ARID2 · rs144431787

See detailed info → Standard

Height (baseline)

near SERPINH1 · rs143717765

See detailed info → Standard

Height (baseline)

near PTHLH · rs142861146

See detailed info → Standard

Height (baseline)

near RNU6-200P · rs142535252

See detailed info → Standard

Height (baseline)

SPI1 · rs141947880

See detailed info → Standard

Height

CSMD3 · rs141856304

See detailed info → Standard

Height (baseline)

near IRAK2 · rs141498975

See detailed info → Standard

Height (baseline)

ARHGEF12 · rs141469382

See detailed info → Standard

Height (baseline)

near IGF1 · rs139221309

See detailed info → Standard

Height (baseline)

BCL10-AS1 · rs138851971

See detailed info → Standard

Height (baseline)

RSRC1 · rs138707981

See detailed info → Standard

Height (baseline)

ZC2HC1C · rs138543059

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Showing 20 of 11479 · page 263 of 574

Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.